Visitor Monitoring Drug Details: TEMODAR
 
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Drug Details

Drug Name: TEMODAR
FDA Application No: (NDA) 021029
Active Ingredient(s): TEMOZOLOMIDE
Company: SCHERING
Original Approval or Tentative Approval Date: August 11, 1999
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
O Orphan drug
 
There are no Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
TEMODAR TEMOZOLOMIDE5MGCAPSULE; ORAL Prescription No None
TEMODAR TEMOZOLOMIDE20MGCAPSULE; ORAL Prescription No None
TEMODAR TEMOZOLOMIDE100MGCAPSULE; ORAL Prescription No None
TEMODAR TEMOZOLOMIDE250MGCAPSULE; ORAL Prescription Yes None
TEMODAR TEMOZOLOMIDE140MGCAPSULE; ORAL Prescription No None
TEMODAR TEMOZOLOMIDE180MGCAPSULE; ORAL Prescription No None


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